chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	10964486	10964486		GTG	13	GENIC	homozygous	128435235
7	10966251	10966252	T	C	25	GENIC	homozygous	115567740
7	10966364	10966365	T	C	24	GENIC	homozygous	115567742
7	10966703	10966704	A	G	33	GENIC	homozygous	115567744
7	10967372	10967373	C	T	40	GENIC	homozygous	116003360
7	10980639	10980639		C	12	GENIC	homozygous	128435239
7	10980752	10980753	G		11	GENIC	homozygous	128435240
7	10980764	10980765	G		11	GENIC	homozygous	128435241
7	10980801	10980802	G	A	5	GENIC	homozygous	133180161
7	10983925	10983926	G	T	27	GENIC	homozygous	116003362
7	10984084	10984097	TGTCTCCCACCCC		18	GENIC	homozygous	128435242
7	10984535	10984536	C	T	25	GENIC	homozygous	116003363
7	10984871	10984871		GCAG	21	GENIC	homozygous	128435244
7	10984879	10984880	C		17	GENIC	homozygous	128435245
7	10984886	10984887	C	T	17	GENIC	homozygous	116003364
7	10984888	10984889	C	G	16	GENIC	homozygous	115567750
7	10984895	10984896	A	G	16	GENIC	homozygous	115567751
7	10984897	10984898	C	G	17	GENIC	homozygous	115567753
7	10986620	10986621	C	T	26	GENIC	homozygous	116003365
7	10968084	10968086	CA		4	GENIC	homozygous	130340575
7	10980863	10980864	T	C	2	GENIC	homozygous	130352556
7	10980874	10980874		G	2	GENIC	homozygous	133486537
7	10984873	10984874	A	G	17	GENIC	homozygous	118306871
7	10984876	10984877	C	G	17	GENIC	homozygous	118306872
7	10984877	10984878	C	G	17	GENIC	homozygous	118306873